OBO ID: DOID:0110711 |
Term Name: | congenital hypotrichosis with juvenile macular dystrophy | Search Ontology: | |
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Synonyms: |
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Definition: | A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the CDH3 gene on chromosome 16q22.1. https://www.ncbi.nlm.nih.gov/pubmed/11544476 | ||
References: |
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Ontology: | Human Disease ( DOID:0110711 ) |
OTHER congenital hypotrichosis with juvenile macular dystrophy PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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CDH3 | Hypotrichosis, congenital, with juvenile macular dystrophy |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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